Stem cells as biological heart pacemakers
- 30 November 2005
- journal article
- review article
- Published by Informa Healthcare in Expert Opinion on Biological Therapy
- Vol. 5 (12) , 1531-1537
- https://doi.org/10.1517/14712598.5.12.1531
Abstract
Abnormalities in the pacemaker function of the heart or in cardiac impulse conduction may result in the appearance of a slow heart rate, traditionally requiring the implantation of a permanent electronic pacemaker. In recent years, a number of experimental approaches have been developed in an attempt to generate biological alternatives to implantable electronic devices. These strategies include, initially, a number of gene therapy approaches (aiming to manipulate the expression of ionic currents or their modulators and thereby convert quiescent cardiomyocytes into pacemaking cells) and, more recently, the use of cell therapy and tissue engineering. The latter approach explored the possibility of grafting pacemaking cells, either derived directly during the differentiation of human embryonic stem cells or engineered from mesenchymal stem cells, into the myocardium. This review will describe each of these approaches, focusing mainly on the stem cell strategies, their possible advantages and shortcomings, as...Keywords
This publication has 35 references indexed in Scilit:
- Genes, stem cells and biological pacemakersCardiovascular Research, 2004
- Human Mesenchymal Stem Cells as a Gene Delivery System to Create Cardiac PacemakersCirculation Research, 2004
- Somatic gene and cell therapy strategies for the treatment of cardiac arrhythmiasAmerican Journal of Physiology-Heart and Circulatory Physiology, 2004
- Biological Pacemaker Implanted in Canine Left Bundle Branch Provides Ventricular Escape Rhythms That Have Physiologically Acceptable RatesCirculation, 2004
- Somatic Gene Transfer and Cardiac Arrhythmias:Journal of Cardiovascular Electrophysiology, 2003
- Biological pacemaker created by gene transferNature, 2002
- Electrophysiological Modulation of Cardiomyocytic Tissue by Transfected Fibroblasts Expressing Potassium ChannelsCirculation, 2002
- Molecular enhancement of porcine cardiac chronotropyHeart, 2001
- Embryonic Stem Cell Lines Derived from Human BlastocystsScience, 1998
- Enhancement of murine cardiac chronotropy by the molecular transfer of the human beta2 adrenergic receptor cDNA.Journal of Clinical Investigation, 1998